Canonical Allele Identifier: PA2741934554
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2780689
ClinVar RCV Id: RCV003659548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Asp124Glu
CA411500270
NM_006941.4:c.372C>G
CA411500277
NM_006941.4:c.372C>A